Background R2* relaxometry's capacity to calculate liver iron concentration (LIC) is limited in patients with severe overload. Hemosiderin increases in these patients, which exhibits a non-monoexponential decay that renders a failed R2* analysis. Purpose/Hypothesis To evaluate a biexponential R2* relaxometry model in children with different ranges of iron overload. Study Type Retrospective. Population In all, 181 children with different conditions associated with iron overload. Field Strength/Sequence 1.5T, T-2*-weighted gradient echo sequence. Assessment Bi- and monoexponential R2* relaxometry were measured in the liver using two regions of interest (ROIs) using a nonproprietary software: one encompassing the whole liver parenchyma (ROI-1) and the other only the periphery (ROI-2). These were drawn by a single trained observer. The residuals for each fitting model were estimated. A ratio between the residuals of the mono- and biexponential models was calculated to identify the best fitting model. Patients with 1) residual ratio >= 1.5 and 2) R2*(fast) >= R2*(slow) were considered as having a predominant biexponential behavior. Statistical Tests Nonparametric tests, Bland-Altman plots, linear correlation, intraclass correlation coefficient. Patients were divided according to their LIC into stable (n = 23), mild (n = 58), moderate (n = 61), and severe (n = 39). Results The biexponential model was more suitable for patients with severe iron overload when compared with the other three LIC categories (P < 0.001) for both ROIs. For ROI-1, 37 subjects met criteria for a predominant biexponential behavior. The slow component (5.7%) had a lower fraction than the fast component (94.2%). For ROI-2, 22 subjects met criteria for a predominant biexponential behavior. The slow component (4.7%) had a lower fraction than the fast component (95.2%). The intraobserver variability between both ROIs was excellent. Data Conclusion The biexponential R2* relaxometry model is more suitable in children with severe iron overload. Technical Efficacy: Stage 1 J. Magn. Reson. Imaging 2019;50:1191-1198.
机构:
Columbia Univ Coll Phys & Surg, Dept Pediat, Div Pediat Hematol, New York, NY 10032 USAColumbia Univ Coll Phys & Surg, Dept Pediat, Div Pediat Hematol, New York, NY 10032 USA
机构:
St Louis Univ, Sch Med, Dept Pediat, St Louis, MO 63103 USA
St Louis Univ, Sch Med, Edward A Doisy Dept Biochem & Mol Biol, St Louis, MO 63103 USASt Louis Univ, Sch Med, Dept Pediat, St Louis, MO 63103 USA
Fleming, Robert E.
;
Ponka, Prem
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机构:
McGill Univ, Jewish Gen Hosp, Lady Davis Inst Med Res, Montreal, PQ H3T 1E2, Canada
McGill Univ, Dept Physiol, Montreal, PQ H3T 1E2, CanadaSt Louis Univ, Sch Med, Dept Pediat, St Louis, MO 63103 USA
机构:
Columbia Univ Coll Phys & Surg, Dept Pediat, Div Pediat Hematol, New York, NY 10032 USAColumbia Univ Coll Phys & Surg, Dept Pediat, Div Pediat Hematol, New York, NY 10032 USA
机构:
St Louis Univ, Sch Med, Dept Pediat, St Louis, MO 63103 USA
St Louis Univ, Sch Med, Edward A Doisy Dept Biochem & Mol Biol, St Louis, MO 63103 USASt Louis Univ, Sch Med, Dept Pediat, St Louis, MO 63103 USA
Fleming, Robert E.
;
Ponka, Prem
论文数: 0引用数: 0
h-index: 0
机构:
McGill Univ, Jewish Gen Hosp, Lady Davis Inst Med Res, Montreal, PQ H3T 1E2, Canada
McGill Univ, Dept Physiol, Montreal, PQ H3T 1E2, CanadaSt Louis Univ, Sch Med, Dept Pediat, St Louis, MO 63103 USA